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Taken together, our qualitative and quantitative analysis of CRISPR- and VNTR-based genotyping methods revealed that both types of markers are characterized by significant amounts of homoplasy.
In breast cancer, established tumor markers are characterized by limited specificity and sensitivity precluding their use for screening and early diagnosis [ 60, 63].
These markers are characterized by the presence of 1 6 nucleotide repeats within the coding and noncoding regions [ 16, 17] of the genome which are codominant, hypervariable, and multiallelic in nature [ 18].
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Cells that were negative for both markers were characterized as viable.
In durum wheat, 9983 putative SNP markers were characterized between their two parents and used for genotyping 91 RILs (van Poecke et al. 2013).
Human adipose mesenchymal stem cells (hAMSCs) were isolated and the cell surface markers were characterized via flow cytometry analysis in addition to multilineage differentiation capacity.
A total of 54 EST-SSR markers were characterized from 120 primer pairs designed by assaying 12 samples of the Vaccinium genus section Cyanococcus.
For the seven Xa genes detected in this study, allele frequency and allele patterns of 24 SNP markers were characterized across the 198 indica panel in correlation to disease reaction to the nine Xoo strains (Additional file 10: Table S4 and Additional file 11: Table S5).
By elucidating possible epistasis between classic T1D loci, major T1D predictive signals (marginal markers) were characterized and fine mapped.
Microsatellite markers were characterized in the extremely specialized ephemeral wetland plant species Cyperus fuscus (Cyperaceae).
Metabolic and cardiovascular markers were characterized in offspring at 13 months of age.
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